IMPPAT Phytochemical information: 
Capsianoside E
Capsianoside E
Summary

SMILES: OCC1OC(OC(CC/C=C(/CC/C=C(/CC/C=C(COC2OC(C)C(C(C2O)OC2OC(COC3OC(C)C(C(C3OC(=O)/C(=C/CC/C(=C/CC/C(=C/CCC(OC3OC(CO)C(C(C3OC3OC(CO)C(C(C3O)O)O)O)O)(C=C)C)/C)/C)/C)O)O)C(C(C2O)O)O)O)/C)C)C)(C=C)C)C(C(C1O)O)OC1OC(CO)C(C(C1O)O)O
InChI: InChI=1S/C82H134O37/c1-13-81(11,118-79-71(63(98)56(91)49(35-85)111-79)116-75-65(100)59(94)54(89)47(33-83)109-75)31-19-28-41(5)23-15-21-39(3)25-17-27-43(7)37-105-74-68(103)69(53(88)46(10)107-74)115-77-67(102)61(96)58(93)51(113-77)38-106-78-70(62(97)52(87)45(9)108-78)114-73(104)44(8)30-18-26-40(4)22-16-24-42(6)29-20-32-82(12,14-2)119-80-72(64(99)57(92)50(36-86)112-80)117-76-66(101)60(95)55(90)48(34-84)110-76/h13-14,21-22,27-30,45-72,74-80,83-103H,1-2,15-20,23-26,31-38H2,3-12H3/b39-21+,40-22+,41-28+,42-29+,43-27-,44-30+
InChIKey: UXMODMFPEVZYRG-JZKHGTLTSA-N
DeepSMILES: OCCOCOCCC/C=C/CC/C=C/CC/C=CCOCOCC)CCC6O))OCOCCOCOCC)CCC6OC=O)/C=C/CC/C=C/CC/C=C/CCCOCOCCO))CCC6OCOCCO))CCC6O))O))O)))))))O))O))))))C=C))C)))))/C)))))/C)))))/C)))))O))O)))))))CCC6O))O))O)))))))O)))))))/C)))))C)))))C)))))C=C))C)))CCC6O))O))OCOCCO))CCC6O))O))O
Scaffold Graph/Node/Bond level: O=C(C=CCCC=CCCC=CCCCOC1OCCCC1OC1CCCCO1)OC1CCCOC1OCC1CCCC(OC2CCOC(OCC=CCCC=CCCC=CCCCOC3OCCCC3OC3CCCCO3)C2)O1
Scaffold Graph/Node level: OC(CCCCCCCCCCCCCOC1OCCCC1OC1CCCCO1)OC1CCCOC1OCC1CCCC(OC2CCOC(OCCCCCCCCCCCCCCOC3OCCCC3OC3CCCCO3)C2)O1
Scaffold Graph level: CC(CCCCCCCCCCCCCCC1CCCCC1CC1CCCCC1)CC1CCCCC1CCC1CCCC(CC2CCCC(CCCCCCCCCCCCCCCCC3CCCCC3CC3CCCCC3)C2)C1
Functional groups: C/C=C(/C)C; C/C=C(C)C; C/C=C(C)C(=O)OC; C=CC; CO; COC(C)OC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like molecules
ClassyFire Class: Fatty Acyls
ClassyFire Subclass: Fatty acyl glycosides
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Diterpenoids
NP Classifier Class: Labdane diterpenoids|Phytane diterpenoids
Synonymous chemical names:
capsianoside e
External chemical identifiers:
CID:118550821; SureChEMBL:SCHEMBL17305084
Chemical structure download
2D:2D MOL2D MOL22D SDF
3D:3D MOL3D MOL23D SDF3D PDB3D PDBQT
Capsianoside E
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 1711.94
Log P RDKit -2.41
Topological polar surface area (Å2) RDKit 580.35
Number of hydrogen bond acceptors RDKit 37
Number of hydrogen bond donors RDKit 21
Number of carbon atoms RDKit 82
Number of heavy atoms RDKit 119
Number of heteroatoms RDKit 37
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 37
Stereochemical complexity RDKit 0.45
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 17
Number of sp3 hybridized carbon atoms RDKit 65
Shape complexity RDKit 0.79
Number of rotatable bonds RDKit 43
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 7
Number of aliphatic rings RDKit 7
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 0
Total number of rings RDKit 7
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 7
Number of saturated rings RDKit 7
Number of Smallest Set of Smallest Rings (SSSR) RDKit 7
Capsianoside E
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 3
Lipinski’s rule of 5 filter RDKit Failed
Number of Ghose filter violations RDKit 4
Ghose filter RDKit Failed
Veber filter RDKit Bad
Pfizer 3/75 filter RDKit Good
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.0172